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Absorption data acquisition

Sample chamber for optical and FTIR studies. For optical and FTIR studies the ambient atmosphere was controlled by placing the sample in vacuum tight chambers described elsewhere (23). These chambers were fitted with optical flats as viewing windows to allow straight throughput for absorption data acquisition and perpendicular obsei— vat ion of emission. The optical flats were sealed by use of 0-r i ngs. [Pg.331]

Phase-sensitive data acquisition NMR data are acquired in this manner so that peaks are recorded with pure absorption-mode or pure dispersionmode line shapes. [Pg.418]

If the areas under the curves are denoted by A, then (based on equal dose) All/Al is the fraction absorbed by oral route. Alll/All is the fraction efficiency of the solid dosage form. The reason for this latter is, of course, that the solid dosage form has to dissolve before the drug contained in it is available for absorption. It is the latter ratio that is important to the investigating pharmaceuticist, and therefore the outcome of the parenteral form is actually not a consideration from a formulation point of view. It is critical overall and if it is low, it may, at the point of parenteral data acquisition, be advisable to stop the program and evaluate the possibility of derivatives that would give better availability. [Pg.190]

Obtain an absorption spectrum of each of your standards, the unknown, and the control sample on a scanning UV-VIS spectrophotometer interfaced to a computer for data acquisition. Follow the instructions provided for your instrument and software. [Pg.234]

Figure 1. Background (no sample) spectrum at different scale expansions illustrating system wavelength response, absorption attributable to typical amounts of residual water and carbon dioxide, and high signal-to-noise. The spectrum required 12 minutes of data acquisition at 8-cm optical retardation. Figure 1. Background (no sample) spectrum at different scale expansions illustrating system wavelength response, absorption attributable to typical amounts of residual water and carbon dioxide, and high signal-to-noise. The spectrum required 12 minutes of data acquisition at 8-cm optical retardation.
Fig. 1. A. Noise level expressed in milli optical density, obtained after 1 minute of data acquisition. B. Time dependent absorption change of the keto group of the primary donor of the bacterial reaction center, at 1685 cm 1 and 1715 cm 1 upon excitation at 600 nm, noise level 30 pOD, measured in the Lissajous scanner. The solid line through the data points is a fit with = 3.8 ps, t2 = 16 ps, t3 = 4 ns and t5 = oc. The time scale is linear up to 3 ps and logarithmic thereafter. Fig. 1. A. Noise level expressed in milli optical density, obtained after 1 minute of data acquisition. B. Time dependent absorption change of the keto group of the primary donor of the bacterial reaction center, at 1685 cm 1 and 1715 cm 1 upon excitation at 600 nm, noise level 30 pOD, measured in the Lissajous scanner. The solid line through the data points is a fit with = 3.8 ps, t2 = 16 ps, t3 = 4 ns and t5 = oc. The time scale is linear up to 3 ps and logarithmic thereafter.
The real and imaginary spectra obtained by Fourier transformation of FID signals are usually mixtures of the absorption and dispersion modes as shown in Fig. 2.13 (a). These phase errors mainly arise from frequency-independent maladjustments of the phase sensitive detector and from frequency-dependent factors such as the finite length of rf pulses, delays in the start of data acquisition, and phase shifts induced by filtering frequencies outside the spectral width A. [Pg.33]

As early as 1978, the possibility of observing VCD via Fourier Transform (FT) interferometric methods was investigated [12], mostly with the goal to improve the signal/noise of the measurement and to reduce data acquisition time. Unfortunately, the advantage of FT-VCD over dispersive VCD has been much smaller than the advantage between FT-IR and dispersive IR absorption spectroscopy. [Pg.100]

Figure 24.14 The left panel is a plan of the testing area near the LENS (reflected shock) tunnel 1 — 8 test section 2 — TDL probe 3 — 4 nozzle M = 8-16 4 — 8" reflected shock tube 5 — fiber optic and signal line conduit 6 — data acquisition and 7 — TDL system optical table. The right panel is a schematic diagram of the setup used to record water-vapor absorption in high-enthalpy flows 1 — InGaAs detectors 2 — tunable diode laser Ai = 1400.74 nm 3 — ring interferometer 4 — tunable diode laser A2 = 1395.69 nm and 5 — HoO reference cell... Figure 24.14 The left panel is a plan of the testing area near the LENS (reflected shock) tunnel 1 — 8 test section 2 — TDL probe 3 — 4 nozzle M = 8-16 4 — 8" reflected shock tube 5 — fiber optic and signal line conduit 6 — data acquisition and 7 — TDL system optical table. The right panel is a schematic diagram of the setup used to record water-vapor absorption in high-enthalpy flows 1 — InGaAs detectors 2 — tunable diode laser Ai = 1400.74 nm 3 — ring interferometer 4 — tunable diode laser A2 = 1395.69 nm and 5 — HoO reference cell...
The experimental equipment requires a standard fine structure X-ray generator operated usually with monochromatic K -radiation. The measurements of the refraction effect are taken by using a commercial small angle X-ray camera of the Kratky type in combination with two scintillation detectors for simultaneous detection of X-ray refraction intensity Ir and sample absorption U- A standard DOS-computer handles the scattering intensity data acquisition and the micromanipulator scanning-system. Figure 1 shows the experimental setup. [Pg.694]


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See also in sourсe #XX -- [ Pg.44 ]




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